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Thora-Seal

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Thora-Seal FDA UDI
Generic Name
Autotransfusion system blood collection container FDA UDI
Device Name
Chest Drainage Unit,Three Chamber System, Collection, Underwater Seal and Suction Control Chambers, Autotransfusion Ready FDA UDI
Model / Reference
8884713176 FDA UDI
Description
Chest Drainage Unit,Three Chamber System, Collection, Underwater Seal and Suction Control Chambers, Autotransfusion Ready FDA UDI

Identifiers

Catalog Number
8884713176 FDA UDI
Primary DI / UDI-DI
20884521074146 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Autotransfusion system blood collection container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Autotransfusion system blood collection container

Thora-Seal by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autotransfusion system blood collection container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 7730d145-63a0-4588-9439-2f1256a95e6b 36 fields · synced May 30, 2026